Device Classification Name |
catheter, percutaneous
|
510(k) Number |
K161126 |
Device Name |
ASAHI Corsair Pro |
Applicant |
ASAHI INTECC CO., LTD. |
1703 WAKITA-CHO, MORIYAMA-KU |
NAGOYA,
JP
463-0024
|
|
Applicant Contact |
CARROLL COUNCILMAN |
Correspondent |
CARDIOMED DEVICE CONSULTANTS, LLC |
5523 RESEARCH PARK DRIVE, SUITE 205 |
BALTIMORE,
MD
21228
|
|
Correspondent Contact |
CANDACE CEDERMAN |
Regulation Number | 870.1250
|
Classification Product Code |
|
Date Received | 04/21/2016 |
Decision Date | 08/25/2016 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|